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Merck
CN

32013

Tebuconazole

PESTANAL®, analytical standard

Synonym(s):

1-(4-Chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)-3-pentanol

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About This Item

Empirical Formula (Hill Notation):
C16H22ClN3O
CAS Number:
Molecular Weight:
307.82
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
403-640-2
MDL number:
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Product Name

Tebuconazole, PESTANAL®, analytical standard

Quality Level

InChI key

UAJBSHCDOPGGBX-UHFFFAOYSA-N

InChI

1S/C16H22ClN3O/c1-15(2,3)16(10-21,20-12-18-11-19-20)9-8-13-4-6-14(17)7-5-13/h4-7,11-12,21H,8-10H2,1-3H3

SMILES string

CC(C)(C)C(CO)(CCc1ccc(Cl)cc1)n2cncn2

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tebuconazole may have been used as reference standard in gas chromatography–mass spectrometry in selected ion monitoring mode (GC/MS, SIM) method for determination of pesticides from Hyptis pectinata, medicinal plant using [Zn(BDC)(H2O)2]n as adsorbent.

General description

Tebuconazole is a triazole fungicide. It is mostly used to control diseases in agricultural crops and is effective against diseases which are soil borne and foliar fungal based.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Coordination polymer adsorbent for matrix solid-phase dispersion extraction of pesticides during analysis of dehydrated Hyptis pectinata medicinal plant by GC/MS.
Aquino A et.al.
Talanta, 83(2), 631-636 (2010)
Shuangyu Song et al.
Journal of agricultural and food chemistry, 66(20), 5031-5038 (2018-01-25)
In this study, a multi-residue analytical method using quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction and dispersive solid-phase extraction (d-SPE) cleanup, followed by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), was investigated for rapid determination of 60 pesticide residues
Hsuan-Chen Wang et al.
Environmental microbiology, 20(1), 270-280 (2017-11-11)
Emerging azole resistance in Aspergillus fumigatus poses a serious threat to human health. This nationwide surveillance study investigated the prevalence and molecular characteristics of azole-resistant A. fumigatus environmental isolates in Taiwan, an island country with increasing use of azole fungicides.
Can Zhang et al.
Frontiers in microbiology, 8, 1779-1779 (2017-10-04)
The genus
Kristina Beijer et al.
Aquatic toxicology (Amsterdam, Netherlands), 198, 73-81 (2018-03-10)
Antifungal azoles are widely used in medicine, agriculture, and material protection and several antifungal azoles have been found in environmental samples. Although these compounds were designed to inhibit fungal enzymes such as lanosterol-14-demethylase (cytochrome P450 (CYP) 51), it is well

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